Preclinical in vitro and in vivo evidence for targeting CD74 as an effective treatment strategy for cutaneous T-cell lymphomas

  • Mariantonia Costanza
  • , Catello Giordano
  • , Ann-Christin von Brünneck
  • , Jing Zhao
  • , Ahmad Makky
  • , Katharina Vinh
  • , Ivonne Aidee Montes-Mojarro
  • , Florian Reisinger
  • , Stephan Forchhammer
  • , Agnieszka Witalisz-Siepracka
  • , Sophie Edtmayer
  • , Dagmar Stoiber
  • , Gang Yin
  • , David Horst
  • , Anja Fischer
  • , Reiner Siebert
  • , Jan P Nicolay
  • , Menghong Yin
  • , Martin Janz
  • , Falko Fend
  • Jürgen C Becker, Christian M Schürch, Lukas Kenner, Chalid Assaf, Olaf Merkel, Stephan Mathas

Research output: Journal article (peer-reviewed)Journal article

Abstract

Background Prognosis and quality of life in patients with advanced cutaneous T-cell lymphoma (CTCL), particularly in those with Sézary syndrome (SS) or advanced-stage mycosis fungoides (MF), are poor. Monoclonal antibodies or antibody–drug conjugates (ADCs) have been added into CTCL treatment algorithms, but the spectrum of antibody-targetable cell surface antigens in T-cell non-Hodgkin lymphomas (T-NHLs) is limited. Objectives To evaluate the expression of the major histocompatibility complex class II chaperone CD74 in common subtypes of CTCL by various methods, and to explore the efficacy of targeting CD74 in CTCL cells with an anti-CD74 ADC in vitro and in vivo. Methods We comprehensively investigated the expression of CD74 in well-defined CTCL cell lines by polymerase chain reaction, immunoblotting and flow cytometry. More than 140 primary CTCL samples of all common subtypes were analysed by immunohistochemistry, flow cytometry, immunofluorescence and ‘co-detection by indexing’ (CODEX) multiplexed tissue imaging, as well as by single-cell RNA sequencing (scRNAseq) analyses. DNA methylation of CTCL cell lines was interrogated by the generation of genome-wide methylation profiling. The effect of a maytansinoid-conjugated humanized ADC against CD74 was investigated in CTCL cell lines in vitro, alone or in combination with gemcitabine, and in vivo after xenotransplantation of CTCL cell lines in NOD-scid Il2rg null mice. Results We demonstrated that CD74 is widely and robustly expressed in CTCL cells. In addition, CD74 expression in SS and MF was confirmed by scRNAseq data analysis and was correlated in CTCL cell lines with CD74 DNA hypomethylation. CD74 was rapidly internalized in CTCL cells and CD74 targeting by the ADC STRO-001 efficiently killed CTCL-derived cell lines. Finally, targeting of CD74 synergized with conventional chemotherapy in vitro and eradicated murine xenotransplants of CTCL cell lines in vivo. Conclusions CD74 is expressed in common CTCL subtypes. Targeting CD74 efficiently killed CTCL cells in vitro and in vivo. We therefore suggest the targeting of CD74 to be a highly promising treatment strategy for CTCL.

Original languageEnglish
Pages (from-to)883-895
Number of pages13
JournalBritish Journal of Dermatology
Volume192
Issue number5
Early online date27 Feb 2025
DOIs
Publication statusPublished - 01 May 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Animals
  • Antigens, Differentiation, B-Lymphocyte/metabolism
  • Cell Line, Tumor
  • DNA Methylation
  • Deoxycytidine/analogs & derivatives
  • Gemcitabine
  • Histocompatibility Antigens Class II/metabolism
  • Humans
  • Immunoconjugates/pharmacology
  • Lymphoma, T-Cell, Cutaneous/drug therapy
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Skin Neoplasms/drug therapy
  • Xenograft Model Antitumor Assays

ASJC Scopus subject areas

  • Dermatology

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